Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency

Hum Mutat. 1997;10(6):430-5. doi: 10.1002/(SICI)1098-1004(1997)10:6<430::AID-HUMU3>3.0.CO;2-H.

Abstract

MHC class II deficiency is a severe primary immunodeficiency characterised by the absence of major histocompatibility complex class II (MHC-II) gene expression. It is genetically heterogeneous and can result from defects in at least four different trans-acting regulatory genes required for transcription of MHC-II genes. One of these genes has recently been shown to encode a novel DNA binding protein called RFX5, which is one subunit of a heteromeric protein complex (RFX) that binds to the promoters of MHC-II genes. We have characterised the mutations in all four patients known to harbour a defect in the RFX5 gene and have mapped this new human disease gene to chromosome 1 band q21, a region frequently exhibiting chromosomal aberrations in a variety of preneoplastic and neoplastic diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping*
  • Chromosomes, Human, Pair 1 / genetics
  • Cloning, Molecular
  • DNA Mutational Analysis*
  • DNA, Complementary / genetics
  • DNA-Binding Proteins / genetics*
  • Female
  • Genes, MHC Class II / genetics*
  • Genetic Carrier Screening
  • Genetic Complementation Test
  • Humans
  • Male
  • Regulatory Factor X Transcription Factors
  • Severe Combined Immunodeficiency / genetics*
  • Transcription Factors / genetics

Substances

  • DNA, Complementary
  • DNA-Binding Proteins
  • RFX5 protein, human
  • Regulatory Factor X Transcription Factors
  • Transcription Factors